Canonical Allele Identifier: CA2621406288

Gene: P2RX4

Linked Data

• gnomAD v4: 12-121222180-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121222182dup , CM000674.2:g.121222182dup	GRCh38
NC_000012.11:g.121659985dup , CM000674.1:g.121659985dup	GRCh37
NC_000012.10:g.120144368dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337233.9:c.427+16dup MANE Select	ENSP00000336607.4:n.427+16dup
ENST00000314442.7:n.4561+16dup
ENST00000337233.8:c.427+16dup	ENSP00000336607.4:n.427+16dup
ENST00000359949.11:c.475+16dup	ENSP00000353032.7:n.475+16dup
ENST00000499638.6:n.479dup
ENST00000538417.2:c.357+16dup
ENST00000538701.5:c.135-6351dup	ENSP00000444033.1:n.135-6351dup
ENST00000540930.5:n.463+16dup
ENST00000541187.5:n.273+16dup
ENST00000542067.5:c.427+16dup	ENSP00000438329.1:n.427+16dup
ENST00000543171.5:c.427+16dup	ENSP00000438131.2:n.427+16dup
ENST00000543318.5:c.427+16dup	ENSP00000444274.1:n.427+16dup
ENST00000543430.5:n.475+16dup
ENST00000543984.5:c.*120+16dup	ENSP00000439386.1:n.*120+16dup
NM_001256796.1:c.475+16dup	NP_001243725.1:n.475+16dup
NM_001261397.1:c.427+16dup	NP_001248326.1:n.427+16dup
NM_001261398.1:c.427+16dup	NP_001248327.1:n.427+16dup
NM_002560.2:c.427+16dup	NP_002551.2:n.427+16dup
NR_046372.1:n.731+16dup
NR_046373.1:n.583+16dup
XM_011538416.1:c.135-6351dup	XP_011536718.1:n.135-6351dup
XM_011538417.1:c.475+16dup	XP_011536719.1:n.475+16dup
XR_944559.1:n.535+16dup
XM_011538416.2:c.135-6351dup	XP_011536718.1:n.135-6351dup
XR_001748726.2:n.481+16dup
XR_001748727.1:n.544+16dup
XR_001748728.1:n.544+16dup
XR_001748729.2:n.481+16dup
XR_944559.2:n.534+16dup
NM_001256796.2:c.475+16dup	NP_001243725.1:n.475+16dup
NM_001261397.2:c.427+16dup	NP_001248326.1:n.427+16dup
NM_001261398.2:c.427+16dup	NP_001248327.1:n.427+16dup
NM_002560.3:c.427+16dup MANE Select	NP_002551.2:n.427+16dup
NR_046372.2:n.463+16dup
NR_046373.2:n.315+16dup